Cargando…
Compounded with hemoglobin Port Phillip and ‐α(4.2) or ‐‐(SEA) deletions were identified in Chinese population
INTRODUCTION: Although over 1000 hemoglobin (Hb) variants were identified so far, Hb Port Phillip compound with α‐thalassemia deletion had no reported before. METHODS: Two patients and the associated families from Guangdong province in China were recruited. Hematological parameters were determined b...
Autores principales: | Du, Li, Bao, Xiuqin, Qin, Danqing, Wang, Jicheng, Yao, Cuize, Liang, Jie, Chen, Jianhong, Yin, Aihua |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8457688/ https://www.ncbi.nlm.nih.gov/pubmed/34398528 http://dx.doi.org/10.1002/mgg3.1699 |
Ejemplares similares
-
Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients
por: Qin, Danqing, et al.
Publicado: (2020) -
Identification of four novel large deletions and complex variants in the α-globin locus in Chinese population
por: Bao, Xiuqin, et al.
Publicado: (2023) -
Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (HBA2:c.178G>C) and Hb Quong Sze (HBA2:c.377T>C)
por: Du, Li, et al.
Publicado: (2021) -
I Phillips
Publicado: (1889) -
I Phillips
Publicado: (1889)